Osteogenic Differentiation of Bone Marrow-Derived Mesenchymal Stem Cells in Electrospun Silica Nonwoven Fabrics

被引:10
作者
Iijima, Kazutoshi [1 ,5 ]
Ishikawa, Shohei [2 ]
Sasaki, Kohei [4 ]
Hashizume, Mineo [1 ]
Kawabe, Masaaki [4 ]
Otsuka, Hidenori [2 ,3 ]
机构
[1] Tokyo Univ Sci, Fac Engn, Dept Ind Chem, Shinjuku Ku, 12-1 Ichigayafunagawara Machi, Tokyo 1620826, Japan
[2] Tokyo Univ Sci, Fac Sci, Grad Sch Sci, Shinjuku Ku, 1-3 Kagurazaka, Tokyo 1628601, Japan
[3] Tokyo Univ Sci, Fac Sci, Dept Appl Chem, Shinjuku Ku, 1-3 Kagurazaka, Tokyo 1628601, Japan
[4] Japan Vilene Co Ltd, 7 Kita Tone, Koga, Ibaraki 3060213, Japan
[5] Yokohama Natl Univ, Fac Engn, Hodogaya Ku, 79-5 Tokiwadai, Yokohama, Kanagawa 2408501, Japan
来源
ACS OMEGA | 2018年 / 3卷 / 08期
关键词
IN-VITRO; STROMAL CELLS; CULTURE; HYDROXYAPATITE; SCAFFOLDS; DESIGN;
D O I
10.1021/acsomega.8b01139
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Silica nonwoven fabrics (SNFs) with enough mechanical strength are candidates as implantable scaffolds. Culture of cells therein is expected to affect the proliferation and differentiation of the cells through cell cell and cell SNF interactions. In this study, we examined three-dimensional (3D) SNFs as a scaffold of mesenchymal stem cells (MSCs) for bone tissue engineering applications. The interconnected highly porous microstructure of 3D SNFs is expected to allow omnidirectional cell cell interactions, and the morphological similarity of a silica nanofiber to that of a fibrous extracellular matrix can contribute to the promotion of cell functions. 3D SNFs were prepared by the sol gel process, and their mechanical properties were characterized by the compression test and rheological analysis. In the compression test, SNFs showed a compressive elastic modulus of over 1 NIPa and a compressive strength of about 200 kPa. These values are higher than those of porous polystyrene disks used for in vitro 3D cell culture. In rheological analysis, the elastic modulus and fracture stress were 3.27 +/- 0.54 kPa and 25.9 +/- 8.3 Pa, respectively. Then, human bone marrow-derived MSCs were cultured on SNFs, and the effects on proliferation and osteogenic differentiation were evaluated. The MSCs seeded on SNF proliferated, and the thiclmess of the cell layer became over 80 mu m after 14 days of culture. The osteogenic differentiation of MSCs on SNFs was induced by the culture in the commercial osteogenic differentiation medium. The alkaline phosphatase activity of MSCs on SNFs increased rapidly and remained high up to 14 days and was much higher than that on two-dimensional tissue culture treated polystyrene. The high expression of RUNX2 and intense staining by alizarin red s after differentiation supported that SNFs enhanced the osteogenic differentiation of MSCs. Furthermore, permeation analysis of SNFs using fluorescein isothiocyanate-dextran suggested a sufficient permeability of SNFs for oxygen, minerals, nutrients, and secretions, which is important for maintaining the cell viability and vitality. These results suggested that SNFs are promising scaffolds for the regeneration of bone defects using MSCs, originated from highly porous and elastic SNF characters.
引用
收藏
页码:10180 / 10187
页数:8
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